Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 50090-7590

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 50090-7590). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Label Image (Lbl500907590)

Metoprolol Succinate 25 mg extended-release film-coated tablets, oral use, manufactured by A-S Medication Solutions. The label shows a package of 30 tablets with each tablet containing 23.75 mg metoprolol succinate, equivalent to 25 mg metoprolol tartrate. Storage instructions indicate keeping at 77 degrees Fahrenheit. The product NDC number 50090-7590 is displayed.*

FDA Label Image

Meto-figure.jpg (Meto Figure)

Forest plot chart showing results for subgroups in the MERIT-HF study. It compares relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure, favoring metoprolol succinate extended-release tablets versus placebo. Subgroups include U.S. and non-U.S. regions, NYHA classes, ejection fraction levels, ischemic etiology, sex, race, prior myocardial infarction, diabetes status, hypertension history, and heart rate categories.*

FDA Label Image

Meto-structure.jpg (Meto Structure)

Chemical structure of metoprolol succinate, showing the molecular arrangement of the active ingredient found in Metoprolol Succinate extended-release tablets.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.